EP3415512A2 - Nouveau composé hétérocyclique et élément électroluminescent organique l'utilisant - Google Patents

Nouveau composé hétérocyclique et élément électroluminescent organique l'utilisant Download PDF

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EP3415512A2
EP3415512A2 EP17867330.7A EP17867330A EP3415512A2 EP 3415512 A2 EP3415512 A2 EP 3415512A2 EP 17867330 A EP17867330 A EP 17867330A EP 3415512 A2 EP3415512 A2 EP 3415512A2
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group
compound
layer
mmol
light emitting
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EP3415512B1 (fr
EP3415512A4 (fr
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Min Woo Jung
Jung Ha Lee
Dong Hoon Lee
Tae Yoon Park
Boon Jae Jang
Seong Mi Cho
Dong Uk Heo
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LG Chem Ltd
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LG Chem Ltd
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Priority claimed from PCT/KR2017/010057 external-priority patent/WO2018084423A2/fr
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    • C07D405/14—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing three or more hetero rings
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    • C07D307/77—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom ortho- or peri-condensed with carbocyclic rings or ring systems
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    • C07D405/02—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings
    • C07D405/04—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings directly linked by a ring-member-to-ring-member bond
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    • C09K2211/00—Chemical nature of organic luminescent or tenebrescent compounds
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    • H10K50/14—Carrier transporting layers
    • H10K50/15—Hole transporting layers
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    • H10K50/165—Electron transporting layers comprising dopants

Definitions

  • the present invention relates to a novel heterocyclic compound and an organic light emitting device comprising the same.
  • an organic light emitting phenomenon refers to a phenomenon where electric energy is converted into light energy by using an organic material.
  • the organic light emitting device using the organic light emitting phenomenon has characteristics such as a wide viewing angle, an excellent contrast, a fast response time, excellent luminance, driving voltage and response speed, and thus many studies have proceeded.
  • the organic light emitting device generally has a structure which comprises an anode, a cathode, and an organic material layer interposed between the anode and the cathode.
  • the organic material layer frequently have a multilayered structure that comprises different materials in order to enhance efficiency and stability of the organic light emitting device, and for example, the organic material layer may be formed of a hole injection layer, a hole transport layer, a light emitting layer, an electron transport layer, an electron injection layer and the like.
  • the holes are injected from an anode into the organic material layer and the electrons are injected from the cathode to the organic material layer, and when the injected holes and the electrons meet each other, an exciton is formed, and light is emitted when the exciton falls to a ground state again.
  • Patent Literature 1 Korean Patent Laid-open Publication No. 10-2000-0051826
  • the present invention provides a compound represented by the following Chemical Formula 1: in Chemical Formula 1,
  • the present invention provides an organic light emitting device comprising a first electrode; a second electrode provided to face the first electrode; and one or more organic material layers provided between the first electrode and the second electrode, wherein one or more of the organic layers includes a compound represented by Chemical Formula 1.
  • the compound represented by Chemical Formula 1 can be used as a material of an organic material layer of an organic light emitting device and can exhibit improved efficiency, a low driving voltage and/or improved lifetime characteristics of the organic light emitting device.
  • the compound represented by Chemical Formula 1 can be used as a hole injection material, a hole transport material, a hole injection and hole transport material, a light emitting material, an electron transport material or an electron injection material.
  • the present invention provides a compound represented by the Chemical Formula 1.
  • substituted or unsubstituted means that substitution is performed by one or more substituent groups selected from the group consisting of deuterium; a halogen group; a nitrile group; a nitro group; a hydroxyl group; a carbonyl group; an ester group; an imide group; an amino group; a phosphine oxide group; an alkoxy group; an aryloxy group; an alkylthioxy group; an arylthioxy group; an alkylsulfoxy group; an arylsulfoxy group; a silyl group; a boron group; an alkyl group; a cycloalkyl group; an alkenyl group; an aryl group; an aralkyl groups; an aralkenyl group; an alkylaryl group; an alkylamine group; an aralkylamine group; a heteroarylamine group; an arylamine group; an arylphosphine oxide group; an alkoxy group
  • substituted group where two or more substituent groups are connected may be a biphenyl group. That is, the biphenyl group may be an aryl group, or may be interpreted as a substituent group where two phenyl groups are connected.
  • the number of carbon atoms in a carbonyl group is not particularly limited, but is preferably 1 to 40 carbon atoms.
  • the carbonyl group may be compounds having the following structures, but is not limited thereto.
  • the ester group may have a structure in which oxygen of the ester group may be substituted by a straight-chain, branched-chain, or cyclic alkyl group having 1 to 25 carbon atoms, or an aryl group having 6 to 25 carbon atoms.
  • the ester group may be compounds having the following structures, but is not limited thereto.
  • the number of carbon atoms in an imide group is not particularly limited but is preferably 1 to 25.
  • the imide group may be compounds having the following structures, but is not limited thereto.
  • the silyl group specifically includes a trimethylsilyl group, a triethylsilyl group, a t-butyldimethylsilyl group, a vinyldimethylsilyl group, a propyldimethylsilyl group, a triphenylsilyl group, a diphenylsilyl group, a phenylsilyl group, and the like, but is not limited thereto.
  • the boron group specifically includes a trimethylboron group, a triethylboron group, a t-butyldimethylboron group, a triphenylboron group, a phenylboron group, and the like, but is not limited thereto.
  • examples of a halogen group include fluorine, chlorine, bromine, or iodine.
  • an alkyl group may be a straight chain or a branched chain, and the number of carbon atoms thereof is not particularly limited but is preferably 1 to 40. According to one embodiment, the alkyl group has 1 to 20 carbon atoms. According to another embodiment, the alkyl group has 1 to 10 carbon atoms. According to still another embodiment, the alkyl group has 1 to 6 carbon atoms.
  • alkyl group examples include methyl, ethyl, propyl, n-propyl, isopropyl, butyl, n-butyl, isobutyl, tert-butyl, sec-butyl, 1-methyl-butyl, 1-ethyl-butyl, pentyl, n-pentyl, isopentyl, neopentyl, tert-pentyl, hexyl, n-hexyl, 1-methylpentyl, 2-methylpentyl, 4-methyl-2-pentyl, 3,3-dimethylbutyl, 2-ethylbutyl, heptyl, n-heptyl, 1-methylhexyl, cyclopentylmethyl, cyclohexylmethyl, octyl, n-octyl, tert-octyl, 1-methylheptyl, 2-ethylhexyl, 2-
  • the alkenyl group may be a straight chain or a branched chain, and the number of carbon atoms thereof is not particularly limited but is preferably 2 to 40. According to one embodiment, the alkenyl group has 2 to 20 carbon atoms. According to another embodiment, the alkenyl group has 2 to 10 carbon atoms. According to still another embodiment, the alkenyl group has 2 to 6 carbon atoms.
  • Specific examples thereof include vinyl, 1-propenyl, isopropenyl, 1-butenyl, 2-butenyl, 3-butenyl, 1-pentenyl, 2-pentenyl, 3-pentenyl, 3-methyl-1-butenyl, 1,3-butadienyl, allyl, 1-phenylvinyl-1-yl, 2-phenylvinyl-1-yl, 2,2-diphenylvinyl-1-yl, 2-phenyl-2-(naphthyl-1-yl)vinyl-1-yl, 2,2-bis(diphenyl-1-yl)vinyl-1-yl, a stilbenyl group, a styrenyl group, and the like, but are not limited thereto.
  • a cycloalkyl group is not particularly limited, but the number of carbon atoms thereof is preferably 3 to 60. According to one embodiment, the cycloalkyl group has 3 to 30 carbon atoms. According to another embodiment, the cycloalkyl group has 3 to 20 carbon atoms. According to another embodiment, the cycloalkyl group has 3 to 6 carbon atoms.
  • cyclopropyl examples thereof include cyclopropyl, cyclobutyl, cyclopentyl, 3-methylcyclopentyl, 2,3-dimethylcyclopentyl, cyclohexyl, 3-methylcyclohexyl, 4-methylcyclohexyl, 2,3-dimethylcyclohexyl, 3,4,5-trimethylcyclohexyl, 4-tert-butylcyclohexyl, cycloheptyl, cyclooctyl, and the like, but are not limited thereto.
  • the aryl group is not particularly limited, but preferably has 6 to 60 carbon atoms, and may be a monocyclic aryl group or a polycyclic aryl group. According to one embodiment, the aryl group has 6 to 30 carbon atoms. According to one embodiment, the aryl group has 6 to 20 carbon atoms.
  • the aryl group may be a phenyl group, a biphenyl group, a terphenyl group or the like as the monocyclic aryl group, but is not limited thereto.
  • polycyclic aryl group examples include a naphthyl group, an anthracenyl group, a phenanthryl group, a pyrenyl group, a perylenyl group, a chrysenyl group, a fluorenyl group or the like, but is not limited thereto.
  • a fluorenyl group may be substituted, and two substituent groups may be bonded to each other to form a spiro structure.
  • the fluorenyl group is substituted, and the like can be formed.
  • the structure is not limited thereto.
  • the heterocyclic group is a heterocyclic group containing one or more of O, N, Si and S as a heteroatom, and the number of carbon atoms thereof is not particularly limited, but is preferably 2 to 60.
  • the heterocyclic group include a thiophene group, a furan group, a pyrrole group, an imidazole group, a triazole group, an oxazole group, an oxadiazole group, a triazole group, a pyridyl group, a bipyridyl group, a pyrimidyl group, a triazine group, an acridyl group, a pyridazine group, a pyrazinyl group, a quinolinyl group, a quinazoline group, a quinoxalinyl group, a phthalazinyl group, a pyridopyrimidinyl group, a pyridopyra
  • the aryl group in the aralkyl group, the aralkenyl group, the alkylaryl group, and the arylamine group is the same as the aforementioned examples of the aryl group.
  • the alkyl group in the aralkyl group, the alkylaryl group and the alkylamine group is the same as the aforementioned examples of the alkyl group.
  • the heteroaryl in the heteroarylamines can be applied to the aforementioned description of the heterocyclic group.
  • the alkenyl group in the aralkenyl group is the same as the aforementioned examples of the alkenyl group.
  • the aforementioned description of the aryl group may be applied except that the arylene is a divalent group.
  • the aforementioned description of the heterocyclic group can be applied except that the heteroarylene is a divalent group.
  • the aforementioned description of the aryl group or cycloalkyl group can be applied except that the hydrocarbon ring is not a monovalent group but formed by combining two substituent groups.
  • the aforementioned description of the heterocyclic group can be applied, except that the heterocycle is not a monovalent group but formed by combining two substituent groups.
  • Chemical Formula 1 is represented by the following Chemical Formula 1-1:
  • all of X are N.
  • Ar 3 is a C 6-60 aryl unsubstituted or substituted with one or more deuterium, or one or more cyano; or a C 2-60 heteroaryl containing at least one heteroatom selected from the group consisting of N, O, S and Si, which is substituted with one or more deuterium, or one or more cyano.
  • Ar 3 is any one selected from the group consisting of: wherein,
  • the organic material layer of the organic light emitting device of the present invention may have a single layer structure, but it may have a multilayered structure in which two or more organic material layers are laminated.
  • the organic light emitting device of the present invention may have a structure including a hole injection layer, a hole transport layer, a light emitting layer, an electron transport layer, an electron injection layer, and the like as the organic material layer.
  • the structure of the organic light emitting device is not limited thereto, but may include a smaller number of organic layers.
  • the organic material layer may include a hole injection layer, a hole transport layer, or a layer simultaneously performing the hole injection and transport, and the hole injection layer, the hole transport layer, or the layer simultaneously performing the hole injection and transport include a compound represented by the Chemical Formula 1.
  • the organic material layer may include an electron transport layer or an electron injection layer, and the electron transport layer or the electron injection layer include a compound represented by the Chemical Formula 1.
  • the electron transport layer, the electron injection layer or a layer simultaneously performing the electron transport and the electron injection include a compound represented by the Chemical Formula 1.
  • the organic material layer may include a light emitting layer and an electron transport layer
  • the electron transport layer may include the compound represented by the Chemical Formula 1.
  • anode material generally, a material having a large work function is preferably used so that holes can be smoothly injected into the organic material layer.
  • the anode material include metals such as vanadium, chrome, copper, zinc, and gold, or an alloy thereof; metal oxides such as zinc oxides, indium oxides, indium tin oxides (ITO), and indium zinc oxides (IZO); a combination of metals and oxides, such as ZnO:AI or SNO 2 :Sb; conductive polymers such as poly(3-methylthiophene), poly[3,4-(ethylene-1,2-dioxy)thiophene] (PEDOT), polypyrrole, and polyaniline, and the like, but are not limited thereto.
  • the compound represented by the Chemical Formula 1 may be included in an organic solar cell or an organic transistor in addition to the organic light emitting device.
  • a glass substrate on which a thin film of ITO (indium tin oxide) was coated in a thickness of 1,300 ⁇ was put into distilled water containing the detergent dissolved therein and washed by the ultrasonic wave.
  • the detergent used herein was a product commercially available from Fisher Co. and the distilled water was one which had been twice filtered by using a filter commercially available from Millipore Co.
  • the ITO was washed for 30 minutes, and washing with ultrasonic waves was then repeated twice for 10 minutes by using distilled water. After the washing with distilled water was completed, the substrate was ultrasonically washed with isopropyl alcohol, acetone, and methanol solvent, and dried, after which it was transported to a plasma cleaner. Then, the substrate was cleaned with oxygen plasma for 5 minutes, and then transferred to a vacuum evaporator.
  • a compound of HI-1 as described below was thermally deposited under vacuum to a thicknesses of 50 ⁇ to form the hole injection layer.
  • the compound of HT-1 was thermally deposited under vacuum to a thicknesses of 250 ⁇ to form a hole transport layer, and a compound of HT-2 was deposited under vacuum to a thickness of 50 ⁇ on the HT-1 vapor deposited layer to form an electron blocking layer.
  • Example 1 On the HT-2 vapor deposited layer, the compound of Example 1 and a phosphorescent dopant YGD-1 were co-deposited at the weight ratio of 88:12 to form a light emitting layer having a thickness of 400 ⁇ .
  • a material of ET-1 was deposited under vacuum to a thickness of 250 ⁇ , and additionally a material of ET-2 was co-deposited with 2% by weight of Li to a thickness of 100 ⁇ to form an electron transport layer and an electron injection layer.
  • Aluminum was deposited on the electron injection layer to a thickness of 1000 ⁇ to form a cathode.
  • the vapor deposition rate of the organic material was maintained at 0.4 to 0.7 ⁇ /sec
  • the deposition rate of aluminum was maintained at 2 ⁇ /sec
  • the degree of vacuum during vapor deposition was maintained at 1 ⁇ 10 -7 ⁇ 5 ⁇ 10 -8 torr.
  • An organic light emitting device was fabricated in the same manner as in Experimental Example 1-1, except that the compound of Example 1, the compound of YGH-1 and the dopant of YGD-1 were co-deposited at the weight of 44:44:12 to form a light emitting layer having a thickness of 400 ⁇ .
  • Example 1 3.5 66 0.46, 0.53 101 1-2
  • Example 2 3.4 73 0.46, 0.52 71 1-3
  • Example 3 3.4 75 0.46, 0.53 72 1-4
  • Example 4 3.4 80 0.47, 0.52 84 1-5
  • Example 5 3.5 74 0.46, 0.52 91 1-6
  • Example 6 3.7 64 0.46, 0.54 70 1-7
  • Example 7 3.6 60 0.46, 0.53 80 1-8
  • Example 8 3.7 74 0.46, 0.54 85 1-9
  • Example 9 3.5 72 0.46, 0.52 67 1-10
  • Example 10 3.5 73 0.46, 0.53 71 1-11
  • Example 11 3.6 58 0.46, 0.53 70 1-12
  • Example 12 3.4 70 0.46, 0.52 71 1-13
  • Example 13 3.5
  • Example 14 3.6 70 0.46, 0.53 64 1-15
  • Example 1 3.8 73 0.46, 0.54 294 1-28
  • Example 2 3.7 75 0.46, 0.54 121 1-29
  • Example 3 3.6 80 0.46, 0.53 183 1-30
  • Example 4 3.9 74 0.46, 0.53 160 1-31
  • Example 5 4.0 60 0.46, 0.52 321 1-32
  • Example 6 3.9 74 0.46, 0.54 202 1-33
  • Example 7 3.8 68 0.46, 0.53 211 1-34
  • Example 8 4.0 70 0.46, 0.52 217 1-35
  • Example 9 3.8 72 0.46, 0.53 197 1-36
  • Example 10 3.7 73 0.46, 0.54 241 1-37
  • Example 11 3.7 66 0.46, 0.53 172 1-38
  • Example 12 3.6 78 0.46, 0.54 145 1-39
  • Example 13 3.6 74 0.46, 0.54 132 1-40
  • Example 14 3.7 77
  • Example 1 and Examples 2 to 4 exhibited a difference in lifetime depending on the substitution positions of dibenzofuran and that the lifetime was improved at a specific position. This tendency was confirmed even in the compounds of Examples 12 to 16. Further, when comparing Examples 1, 5, 6, 7, 8, 9, 10, 11, 18, and 19, it could be seen that they exhibited the difference in efficiency characteristics depending on the substituent types and substitution positions of R in the Chemical Formula 1, and that they were materials superior in terms of the efficiency, voltage and lifetime.
  • Comparative Examples 3 to 5 it could be seen that they exhibited the difference in efficiency and lifetime depending on the number of R and the bond length of R.
  • Comparative Examples 6 to 12 and 18 it could be confirmed that the characteristics were also varied depending on this tendency and the difference in the state of bonding with the electron deficient group.
  • Comparative Examples 13 to 17 it was confirmed that even when one substituent was present, the efficiency, lifetime and the like were varied depending on the type of the substituent.
  • the compounds of the present invention exhibited excellent properties in terms of efficiency and lifetime due to the difference in the number of substituents and the degree of bonding, as compared with the compounds of the Comparative Examples.
  • a glass substrate on which a thin film of ITO (indium tin oxide) was coated in a thickness of 1,300 ⁇ was put into distilled water containing the detergent dissolved therein and washed by the ultrasonic wave.
  • the detergent used herein was a product commercially available from Fisher Co. and the distilled water was one which had been twice filtered by using a filter commercially available from Millipore Co.
  • the ITO was washed for 30 minutes, and washing with ultrasonic waves was then repeated twice for 10 minutes by using distilled water. After the washing with distilled water was completed, the substrate was ultrasonically washed with isopropyl alcohol, acetone, and methanol solvent, and dried, after which it was transported to a plasma cleaner. Then, the substrate was cleaned with oxygen plasma for 5 minutes, and then transferred to a vacuum evaporator.
  • a compound of HI-1 as described below was thermally deposited under vacuum to a thicknesses of 50 ⁇ to form the hole injection layer.
  • the compound of HT-1 was thermally deposited under vacuum to a thicknesses of 800 ⁇ and a compound of HT-3 was sequentially vacuum-deposited thereon to a thickness of 500 ⁇ to form a hole transport layer.
  • the compound of Example 1, GH1 and a phosphorescent dopant GD-1 were co-deposited at the weight ratio of 47.5:47.5:5 to form a light emitting layer having a thickness of 400 ⁇ .
  • a material of ET-3 was vacuum-deposited to a thickness of 50 ⁇ to form a hole blocking layer.
  • a material of ET-4 and LiQ were co-deposited at the weight ratio of 1:1 to form an electron transport layer having a thickness of 250 ⁇ .
  • sequentially lithium fluoride (LiF) was deposited to a thickness of 10 ⁇ , and aluminum was deposited thereon to a thickness of 1000 ⁇ to form a cathode.
  • the vapor deposition rate of the organic material was maintained at 0.4 to 0.7 ⁇ /sec
  • the deposition rate of the lithium fluoride of the cathode was maintained at 0.3 ⁇ /sec and that of aluminum was maintained at 2 ⁇ /sec
  • the degree of vacuum during vapor deposition was maintained at 1 ⁇ 10 -7 ⁇ 5 ⁇ 10 -8 torr.
  • V Compound Voltage (V)(@10mA/c m 2 ) Efficiency (Cd/A) (@10mA/cm 2 ) Color coordinate (x,y) Lifetime (h) T95 at 50mA/cm 2 2-1
  • Example 1 4.4 64 0.34, 0.61 241 2-2
  • Example 2 4.3 65 0.33, 0.63 155 2-3
  • Example 3 4.2 66 0.34.
  • Example 4 4.4 63 0.34, 0.63 181 2-5
  • Example 5 4.8 50 0.37, 0.67 241 2-6
  • Example 6 4.6 67 0.34, 0.61 191 2-7
  • Example 7 4.4 59 0.34, 0.60 118 2-8
  • Example 8 4.2 64 0.35, 0.61 101 2-9
  • Example 9 4.3 65 0.34, 0.61 117 2-10
  • Example 10 4.4 65 0.35, 0.62 197 2-11
  • Example 11 4.3 61 0.33, 0.62 142 2-12
  • Example 12 4.4 66 0.34, 0.62 129 2-13
  • Example 13 4.3 67 0.33, 0.61 131 2-14
  • Example 14 4.4 65 0.34, 0.62 133 2-15
  • Example 15 4.3 64 0.31, 0.63 142 2-16
  • Example 16 4.3 61 0.30, 0.64 160 2-17
  • Example 17 4.4 62 0.33, 0.62 181 2-18
  • Example 18 4.4 61 0.34, 0.63 197 2-19
  • Example 19 4.5 63 0.
  • a glass substrate on which a thin film of ITO (indium tin oxide) was coated in a thickness of 1,000 ⁇ was put into distilled water containing a dispersant dissolved therein and washed by the ultrasonic wave.
  • the detergent used herein was a product commercially available from Fisher Co. and the distilled water was one which had been twice filtered by using a filter commercially available from Millipore Co.
  • the ITO was washed for 30 minutes, and washing with ultrasonic waves was then repeated twice for 10 minutes by using distilled water. After the washing with distilled water was completed, the substrate was ultrasonically washed in the order of isopropyl alcohol, acetone, and methanol solvent, and dried,
  • a compound of HI-1 was thermally deposited under vacuum to a thicknesses of 500 ⁇ to form the hole injection layer.
  • the compound of HT-1 was deposited under vacuum to a thicknesses of 400 ⁇ to form a hole transport layer.
  • a material of H1 and a dopant D1 compound (2.5 wt%) was deposited under vacuum to a thickness of 300 ⁇ .
  • a compound of ET-A below was vacuum-deposited on the light emitting layer to a thickness of 50 ⁇ to form an a-electron transport layer.
  • Example 1 On the a-electron transport layer, the compound of Example 1 and the LiQ (lithium fluoride) were vacuum-deposited at the weight ratio of 1:1 to form an electron injection and transport layer having a thickness of 350 ⁇ . On the electron injection and transport layer, sequentially, lithium fluoride (LiF) was deposited to a thickness of 12 ⁇ , and aluminum was deposited thereon to a thickness of 2000 ⁇ to form a cathode.
  • LiF lithium fluoride
  • the vapor deposition rate of the organic material was maintained at 0.4 to 0.7 ⁇ /sec
  • the deposition rate of the lithium fluoride of the cathode was maintained at 0.3 ⁇ /sec and that of aluminum was maintained at 2 ⁇ /sec
  • the degree of vacuum during vapor deposition was maintained at 2 ⁇ 10 -7 ⁇ 5 ⁇ 10 -6 torr.
  • a preliminary mixture was prepared by using Example 16 and CoH1 compound at a weight ratio of 5: 5, and then these were physically mixed, pulverized and then loaded in an evaporation source.
  • the premixed composition was thermally co-evaporated at a rate of 2 ⁇ /sec in a vacuum chamber under a pressure of less than 10 -7 torr and deposited on a glass substrate. While the evaporation and cooling of the source were not stopped, the substrate was successively replaced after deposition of a film having a thickness of 500 ⁇ .
  • the composition of the film was analyzed by high performance liquid chromatography (HPLC), and the results are shown in Table 8 below.
  • the deposition rate of the composition could be varied upon co-deposition with deuterium.
  • substrate 2 anode 3: light emitting layer 4: cathode 5: hole injection layer 6: hole transport layer 7: light emitting layer 8: electron transport layer

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  • Electroluminescent Light Sources (AREA)
  • Plural Heterocyclic Compounds (AREA)
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EP4056566A4 (fr) * 2019-11-06 2023-10-18 LT Materials Co., Ltd. Composé hétérocyclique, diode électroluminescente organique le comprenant, composition pour couche de matière organique de diode électroluminescente organique, et procédé de fabrication de diode électroluminescente organique
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